Searching journal content for articles similar to Alexeyenko and Sonnhammer 19 (6): 1107.

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  1. ...isoform profiling workflow based on long-read sequencing. Our focus was on Pteromalus puparum, a representative parasitoid wasp species with a global distribution. By analyzing the isoform landscape of venom genes, along with gene/isoform expression and venom proteome data, we aimed to elucidate the role...
  2. ...Tyrosine 1–phosphorylated RNA polymerase II transcribes PROMPTs to facilitate proximal promoter pausing and induce global transcriptional repression in response to DNA damage Kamal Ajit1, Adele Alagia1, Kaspar Burger2,3 and Monika Gullerova1 1Sir William Dunn School of Pathology, Oxford, OX1 3RE...
  3. ...of each genomic locus to all other genomic loci by integrating k-step (k = 1, 2, 3, ……) transition probability matrices derived from a Hi-C contact matrix (see Methods). Taking all other genomic loci into consideration, the diffusion property is hence defined based on global information of the Hi...
  4. ...and silencing-complex maturation. Within Argonaute, guide strands have stabilities that vary by 100-fold. Half-lives also vary globally between cell lines, with median values ranging from 11 to 34 h in mESCs and contact-inhibited MEFs, respectively. Moreover, relative half-lives for individual miRNAs vary...
  5. ..., there remains much to be understood about the splicing factors and the cis sequence elements controlling tissue and neuron subtype-specific splicing patterns. By using translating ribosome affinity purification coupled with deep-sequencing (TRAP-seq) in Caenorhabditis elegans, we have obtained high coverage...
  6. ...(Wahl et al. 2009). Global short-read sequencing (RNA-seq) of nascent RNA from yeast to human has revealed that most introns are removed from pre-mRNA during transcription by RNA polymerase II (Pol II) (Brugiolo et al. 2013). Therefore, spliceosome assembly and splicing occur on nascent RNA...
  7. ...(cluster 4). Moreover, the cancer networks (clusters 2 and 4) are clearly separated from the corresponding healthy tissues (cluster 5), suggesting that distinct coupling patterns characterize healthy and cancer tissues. In particular, the flux coupling profiles of all nine considered eukaryotes form...
  8. ...partially. For example, the core 3′ end processing factor FIP1L1 can bind poly(U) (Kaufmann et al. 2004; Lackford et al. 2014), and its knock-down causes a systematic increase in 3′ UTR lengths (Lackford et al. 2014; Li et al. 2015). HNRNPC knock-down causes global changes in alternative cleavage...
  9. ...to be comprehensively described. To elucidate the complete set of alterations in these factors and how they globally affect alternative splicing that may contribute to cancer, we analyzed RNA and DNA sequencing data from The Cancer Genome Atlas (TCGA) project for 11 solid tumor types.ResultsRBPs are frequently de...
  10. ..., such global counting is not particularly illuminating as lineages vastly differ in their gain and loss patterns, and, furthermore, these patterns are hardly uniform in time. In the following, we analyze the comparative contributions of intron gains and losses in different parts of the eukaryotic tree and...
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